Elizabeth Ormondroyd

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 13

Top Topics

Cross Sectional

Top Venues

European journal of human genetics : EJHG

Circulation. Genomic and precision medicine

European journal of cancer care

Nature genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Elizabeth Ormondroyd, Christopher Grace, Wendy Borsari, Anuj Goel, Barbara McDonough, Joel Rose, Christine E Seidman, Hugh C Watkins
Genetic therapies for cardiomyopathy: survey of attitudes of the patient community for the CureHeart project. European journal of human genetics : EJHG 32 (9) (2024)
Elizabeth Ormondroyd, Christopher Grace, Wendy Borsari, Anuj Goel, Barbara McDonough, Joel Rose, Christine E Seidman, Hugh C Watkins
Genetic therapies for cardiomyopathy: survey of attitudes of the patient community for the CureHeart project. European journal of human genetics : EJHG (2024)
Danya F Vears, Nina Hallowell, Heidi Beate Bentzen, Bridget Ellul, Therese Haugdahl Nøst, Angeliki Kerasidou, Shona M Kerr, Michaela Th Mayrhofer, Signe Mezinska, Elizabeth Ormondroyd, Berge Solberg, Birgitte Wirum Sand, Isabelle Budin-Ljøsne
A practical checklist for return of results from genomic research in the European context. European journal of human genetics : EJHG (2023)
Joshua J Nolan, Elizabeth Ormondroyd
Direct-to-consumer genetic tests providing health risk information: A systematic review of consequences for consumers and health services. Clinical genetics (2023)
Kate L Thomson, Elizabeth Ormondroyd
The Genetic Basis of Primary Cardiomyopathies in Childhood: Implications for Clinical Genetic Testing. Circulation. Genomic and precision medicine (2022)
Belinda Rahman, Alastair Lamb, Andrew Protheroe, Ketan Shah, Joyce Solomons, Jonathan Williams, Elizabeth Ormondroyd
Genomic sequencing in oncology: Considerations for integration in routine cancer care. European journal of cancer care 31 (3) (2022)
Andrew R Harper, Anuj Goel, Christopher Grace, Kate L Thomson, Steffen Erhard Petersen, Xiao Xu, Adam Waring, Elizabeth Ormondroyd, Christopher M Kramer, Carolyn Y Ho, Stefan Neubauer, null null, Rafik Tadros, James Simon Ware, Connie R Bezzina, Martin Farrall, Hugh C Watkins
Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity. Nature genetics 53 (2) (2021)
Ryan M Baxley, Wendy Leung, Megan M Schmit, Jacob Peter Matson, Lulu Yin, Marissa K Oram, Liangjun Wang, John Taylor, Jack Hedberg, Colette B Rogers, Adam J Harvey, Debashree Basu, Jenny C Taylor, Alistair T Pagnamenta, Helene Dreau, Jude Craft, Elizabeth Ormondroyd, Hugh C Watkins, Eric A Hendrickson, Emily M Mace, Jordan S Orange, Hideki Aihara, Grant S Stewart, Edward Blair, Jeanette Gowen Cook, Anja-Katrin Bielinsky
Bi-allelic MCM10 variants associated with immune dysfunction and cardiomyopathy cause telomere shortening. Nature communications 12 (1) (2021)
Julian O M Ormerod, Elizabeth Ormondroyd, Yanhui Li, John Taylor, Jinhong Wei, Wenting Guo, Ruiwu Wang, Caroline N S Sarton, Karen McGuire, Helene M P Dreau, Jenny C Taylor, Matthew R Ginks, Kim Rajappan, S R Wayne Chen, Hugh C Watkins
Provocation Testing and Therapeutic Response in a Newly Described Channelopathy: RyR2 Calcium Release Deficiency Syndrome. Circulation. Genomic and precision medicine 15 (1) (2021)
Elizabeth Ormondroyd, Peter Border, Judith Hayward, Andrew Papanikitas
Genomic health data generation in the UK: a 360 view. European journal of human genetics : EJHG (2021)
Elizabeth Ormondroyd, Andrew R Harper, Kate L Thomson, Michael P Mackley, Jennifer Martin, Christopher J Penkett, Silvia Salatino, Hannah Stark, Jonathan Stephens, Hugh C Watkins
Secondary findings in inherited heart conditions: a genotype-first feasibility study to assess phenotype, behavioural and psychosocial outcomes. European journal of human genetics : EJHG 28 (11) (2020)
James Buchanan, Edward Blair, Kate L Thomson, Elizabeth Ormondroyd, Hugh Watkins, Jenny C Taylor, Sarah Wordsworth
Do health professionals value genomic testing? A discrete choice experiment in inherited cardiovascular disease. European journal of human genetics : EJHG 27 (11) (2019)
Michael P Mackley, Edward Blair, Michael Parker, Jenny C Taylor, Hugh Watkins, Elizabeth Ormondroyd
Views of rare disease participants in a UK whole-genome sequencing study towards secondary findings: a qualitative study. European journal of human genetics : EJHG 26 (5) (2018)